DANVERS, Mass.--(BUSINESS WIRE)--NeuroLogica Corporation announced today it has received CE Mark approval for its most recent product BodyTom™, a portable, full body, multi-slice CT scanner. CE Mark approval allows BodyTom ™ to be sold in the European Union.
NeuroLogica’s BodyTom™ is a completely portable, full body, 32 slice CT that boasts an impressive 85cm gantry and 60cm field of view (FOV). The battery powered BodyTom™ can be easily transported from room to room, similar to the widely used portable chest X-ray systems. Its unique capabilities provide high quality CT images wherever needed, including the clinic, ICU, OR and Emergency/Trauma Department. BodyTom™ is DICOM 3.1 compliant and compatible with all PACS, surgical navigation, electronic medical records, and planning systems. BodyTom™ is the newest offering in NeuroLogica’s portable computed tomography imaging line.
“Achieving the CE Mark on our BodyTom™ represents a significant milestone and achievement by all of the employees of our company,” said Dr. Eric Bailey, President and CEO for NeuroLogica Corporation. “The certification signifies that we have met the rigorous clinical, quality, and performance requirements of the EU authorities and demonstrates the commitment we have to our future customers.”
For more information on the BodyTom™ full body portable CT scanner, please contact Hon Jin Chang at 1-978-564-8520 or by email, hchang@neurologica.com.
About NeuroLogica Corporation
Located in Danvers, Massachusetts, NeuroLogica Corporation (www.neurologica.com) specializes in the design and manufacture of cutting edge imaging equipment that is easy to use and brings the power of imaging to the patient wherever they may be. NeuroLogica’s BodyTom™ CT and CereTom® CT are FDA registered and the quality system is certified to ISO 13485:2003 and ISO 9001:2008 with Canadian Medical Device Amendments. NeuroLogica’s BodyTom™ CT and CereTom® CT are CE marked (European Conformity) for distribution in the European Union and European Economic Area.